vardenafil hydrochloride
Generic: vardenafil hydrochloride
Labeler: avkareDrug Facts
Product Profile
Brand Name
vardenafil hydrochloride
Generic Name
vardenafil hydrochloride
Labeler
avkare
Dosage Form
TABLET
Routes
Active Ingredients
vardenafil hydrochloride 10 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42291-847
Product ID
42291-847_4875c23d-91ea-f449-e063-6394a90a5a74
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209057
Listing Expiration
2027-12-31
Marketing Start
2019-01-31
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291847
Hyphenated Format
42291-847
Supplemental Identifiers
RxCUI
UPC
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
vardenafil hydrochloride (source: ndc)
Generic Name
vardenafil hydrochloride (source: ndc)
Application Number
ANDA209057 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/1
Packaging
- 30 TABLET in 1 BOTTLE (42291-847-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4875c23d-91ea-f449-e063-6394a90a5a74", "openfda": {"upc": ["0342291847309", "0342291848306"], "unii": ["5M8S2CU0TS"], "rxcui": ["349479", "349480"], "spl_set_id": ["80c4793d-e19e-10f0-e053-2991aa0a4620"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (42291-847-30)", "package_ndc": "42291-847-30", "marketing_start_date": "20190131"}], "brand_name": "Vardenafil Hydrochloride", "product_id": "42291-847_4875c23d-91ea-f449-e063-6394a90a5a74", "dosage_form": "TABLET", "pharm_class": ["Phosphodiesterase 5 Inhibitor [EPC]", "Phosphodiesterase 5 Inhibitors [MoA]"], "product_ndc": "42291-847", "generic_name": "Vardenafil Hydrochloride", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vardenafil Hydrochloride", "active_ingredients": [{"name": "VARDENAFIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA209057", "marketing_category": "ANDA", "marketing_start_date": "20190131", "listing_expiration_date": "20271231"}